Active Ingredient: SINCALIDE
Proprietary Name: KINEVAC
Dosage Form; Route of Administration: POWDER; INTRAVENOUS
Strength: 0.005MG/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N017697
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRACCO DIAGNOSTICS INC
Marketing Status:
Prescription
Patent and Exclusivity Information